Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29770 | A01 | 18844139 | C | T | downstream_gene_variant | MODIFIER | c.*1290G>A| |
S273 |
2 | BAA01g29770 | A01 | 18845478 | G | A | missense_variant&splice_region_variant | MODERATE | c.1670C>T|p.Ala557Val |
S58 |
3 | BAA01g29770 | A01 | 18845866 | C | T | missense_variant | MODERATE | c.1483G>A|p.Ala495Thr |
S255 |
4 | BAA01g29770 | A01 | 18845982 | G | A | missense_variant | MODERATE | c.1441C>T|p.Pro481Ser |
S286 |
5 | BAA01g29770 | A01 | 18846347 | G | A | splice_region_variant&intron_variant | LOW | c.1166+8C>T| |
S151 |
6 | BAA01g29770 | A01 | 18846712 | C | T | missense_variant | MODERATE | c.809G>A|p.Arg270His |
S82 S92 |
7 | BAA01g29770 | A01 | 18847652 | C | T | missense_variant | MODERATE | c.293G>A|p.Gly98Glu |
S20 |
8 | BAA01g29770 | A01 | 18847859 | G | A | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S225 S73 |
9 | BAA01g29770 | A01 | 18848170 | C | T | upstream_gene_variant | MODIFIER | c.-226G>A| |
S289 S290 |
10 | BAA01g29770 | A01 | 18848859 | C | T | upstream_gene_variant | MODIFIER | c.-915G>A| |
S295 |
11 | BAA01g29770 | A01 | 18850009 | A | T | upstream_gene_variant | MODIFIER | c.-2065T>A| |
S292 |